A new analytical method to diagnose congenital myasthenia with stimulated single-fiber electromyography
Author:
Publisher
Wiley
Subject
Physiology (medical),Cellular and Molecular Neuroscience,Clinical Neurology,Physiology
Reference19 articles.
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4. A ?-subunit mutation in the acetylcholine receptor channel gate causes severe slow-channel syndrome
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5. Electrophysiological study of neuromuscular junction in congenital myasthenic syndromes, congenital myopathies, and chronic progressive external ophthalmoplegia;Neuromuscular Disorders;2020-11
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